참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | Phenylmethyl 2-(2,5-dioxoimidazolidinyl)acetate | HCID 22574607 | — |
| 반응물 | 2-Propanol, 2-methyl-, lithium salt (1:1) | HCID 23664764 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Phenylmethyl 2-(2,5-dioxo-3-benzylimidazolidinyl)acetate | HCID 22574604 | 62.8% |
반응 단계
To a solution of phenylmethyl 2-(2,5-dioxoimidazolidinyl)acetate (4.0 g, 16.1 mmol) in DMF (50 ml) at 0° C. were added lithium tert-butoxide (1.6 g, 19.3 mmol) and benzyl bromide (2.1 ml, 17.7 mmol). After stirring the mixture at room temperature overnight, the reaction mixture was poured into water (100 ml) and the mixture was extracted with ethyl acetate. The organic phase was washed with water, 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate solution and brine. The organic solution was dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was purified by column chromatography (silica gel, n-hexane:ethyl acetate=3:1) to give phenylmethyl 2-(2,5-dioxo-3-benzylimidazolidinyl)acetate (3.42 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06852744B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-4c3084a0cf56463b889bd6bdadaadc60 |
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| 출처 메모 | uspto-grants-2005_02 |
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